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Am J Physiol Gastrointest Liver Physiol 292: G39-G52, 2007. First published August 3, 2006; doi:10.1152/ajpgi.00181.2006
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LIVER AND BILIARY TRACT

Morphogenic protein epimorphin protects intestinal epithelial cells from oxidative stress by the activation of EGF receptor and MEK/ERK, PI3 kinase/Akt signals

Masahiro Iizuka,1 Kenji Sasaki,1 Yohei Hirai,2 Kenichi Shindo,1 Shiho Konno,1 Hiroaki Itou,1 Shigetoshi Ohshima,1 Yasuo Horie,1 and Sumio Watanabe1

1Department of Internal Medicine, Akita University School of Medicine, Akita; 2Department of Morphoregulation, Institute for Frontier Medical Science, Kyoto University, Kyoto, Japan

Submitted 30 April 2006 ; accepted in final form 16 July 2006

Epimorphin is a mesenchymal protein that regulates morphogenesis of epithelial cells. Our preliminary study suggested a novel function of epimorphin in enhancing survival of intestinal epithelial cells (IEC). Oxidative stress leads to cell injury and death and is suggested to be a key contributor to pathogenesis of inflammatory bowel disease. This study was conducted to determine whether epimorphin protects IEC from oxidative stress. Rat intestinal epithelial cell line IEC-6 was cultured with epimorphin (10 and 20 µg/ml), and the life span of IEC was assessed. The mean life span of IEC-6 cells was prolonged 1.9-fold (P < 0.0006) by treatment with epimorphin. We then examined the epimorphin signaling pathways. Epimorphin phosphorylated epidermal growth factor (EGF) receptor, activated the MEK/extracellular signal-regulated kinase 1/2 mitogen-activated protein kinase and phosphatidylinositol 3 (PI3) kinase/Akt pathways, phosphorylated Bad, and induced Bcl-XL and survivin. Hydrogen peroxide (1 mM) induced cell death in 92% of IEC-6 cells, but epimorphin dramatically diminished (88.7%) cell death induced by hydrogen peroxide (P < 0.0001). This protective effect of epimorphin was significantly attenuated by inhibitors of MEK and PI3 kinase (P < 0.0001) or EGF receptor-neutralizing antibody (P = 0.0007). In wound assays, the number of migrated cells in the wound area decreased (72.5%) by treatment with 30 µM hydrogen peroxide, but epimorphin increased the number of migrated cells 3.18-fold (P < 0.0001). These results support a novel function of epimorphin in protecting IEC from oxidative stress. This anti-oxidative function of epimorphin is dramatic and is likely mediated by the activation of EGF receptors and the MEK/extracellular signal-regulated kinase and PI3 kinase/Akt signaling pathways and through the induction of anti-apoptotic factors.

epimorphin; oxidative stress; intestinal epithelial cells; epidermal growth factor receptor; extracellular signal-regulated kinase



Address for reprint requests and other correspondence: M. Iizuka, Dept. of Internal Medicine, Akita Univ. School of Medicine, 1-1-1 Hondo, Akita 010-8543, Japan (e-mail: maiizuka{at}doc.med.akita-u.ac.jp)




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